Clinically unsuspected bilateral malignant pheochromocytoma.

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dc.contributor.authorPowari, Manishen_US
dc.contributor.authorRajesh, Logasundaramen_US
dc.contributor.authorJoshi, Kusumen_US
dc.date.accessioned2007-04-22en_US
dc.date.accessioned2009-05-29T12:16:26Z
dc.date.available2007-04-22en_US
dc.date.available2009-05-29T12:16:26Z
dc.date.issued2007-04-22en_US
dc.description.abstractPheochromocytoma is an uncommon tumor and occurrence of bilateral malignant tumor is extremely rare. Labile hypertension is the common presenting feature of pheochromocytomas. Herein we describe one such case ofbilateral malignant pheochromocytoma, which was clinically silent except for pain and mass in hypochondrium. Histopathology showed features of malignancy along with hyaline globules, which are less described with malignant tumors. Electron microscopy showed neurosecretory granules in tumor cells.en_US
dc.description.affiliationDepartment of Histopathology, Post Graduate Institute of Medical Education & Research, Chandigarh-160 012.en_US
dc.identifier.citationPowari M, Rajesh L, Joshi K. Clinically unsuspected bilateral malignant pheochromocytoma. Indian Journal of Pathology & Microbiology. 2007 Apr; 50(2): 313-4en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/74415
dc.language.isoengen_US
dc.source.urihttps://www.ijpmonline.orgen_US
dc.subject.meshAdrenal Gland Neoplasms --diagnosisen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMicroscopy, Electron, Transmissionen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshNeoplasms, Multiple Primary --diagnosisen_US
dc.subject.meshPheochromocytoma --diagnosisen_US
dc.subject.meshSecretory Vesicles --ultrastructureen_US
dc.titleClinically unsuspected bilateral malignant pheochromocytoma.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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